NZ541681A

NZ541681A - Treatment of bacterial diseases of the respiratory organs by locally applying ciprofloxacin and its salts

Info

Publication number: NZ541681A
Application number: NZ541681A
Authority: NZ
Inventors: Rainer Endermann; Harald Labischinski; Christoph Ladel; Uwe Petersen; Ben Newton
Original assignee: Bayer Healthcare Ag
Priority date: 2003-02-10
Filing date: 2004-01-28
Publication date: 2009-02-28
Also published as: IL170027A; MXPA05008407A; TW200503716A; TWI347843B; EP1594500B1; NO20054180L; AU2004210399B2; UY28179A1; DK1594500T3; JP4828405B2; AR043117A1; RU2373937C2; PE20050189A1; ATE482706T1; US8034817B2; CA2515262C; RU2373937C9; ECSP055959A; HRP20050786B1; AU2004210399A1

Abstract

Disclosed is a method for controlling bacterial diseases of the respiratory organs in non-human animals by local administration of an antibacterially effective amount of solid ciprofloxacin of the formula (III) wherein R=H.

Description

<div class="application article clearfix" id="description"> New Zealand Paient Spedficaiion for Paient Number 541 681 WO 2004/069253 5^1681 l PCT/EP2004/000710 10 TREATMENT OF BACTERIAL DISEASES OF THE RESPIRATORY ORGANS BY LOCALLY APPLYING FLUOROQUINOLONES The present invention relates to the use of dosage forms which contain quinolonecarboxylic acid derivatives and enable local treatment of diseases of the respiratory organs, in particular lung diseases caused by bacteria. Despite enormous progress in the area of controlling bacterial infectious diseases through the introduction of various classes of antibiotics in the last 70 years, severe lung infections still represent an important problem, especially in relation to pathological states such as cystic fibrosis, bronchiectasis and increasingly also chronic obstructive pulmonary diseases (COPD), which are associated with infections which can be treated only with difficulty or not at all. Active ingredients from the class of fluoroquinolones, especially also moxifloxacin and ciprofloxacin, are frequently employed for the treatment of such diseases because of their relevant range of antibacterial effects and their bactericidal action. Moxifloxacin hydrochloride (I) 15 20 25 x HCI o o cn & O W o -r* ru O * (I) is an antibacterial active ingredient from the class of quinolonecarboxylic acid derivatives for the treatment and prevention of otitis, pharyngitis, pneumonia, peritonitis, pyelonephritis, cystitis, endocarditis, systemic infections, acute and chronic bronchitis, septic infections, diseases of the upper airways, diffuse panbronchiolitis, pulmonary emphysema, dysentery, enteritis, liver abscesses, urethritis, prostatitis, epididymitis, gastrointestinal infections, bone and joint infections, cystic fibrosis, skin infections, postoperative wound infections, abscesses, phlegmons, wound infections, infected burns, burns, infections in the oral region, infections after dental operations, osteomyelitis, septic arthritis, cholecystitis, peritonitis with appendicitis, cholangitis, intraabdominal abscesses, pancreatitis, sinusitis, mastoiditis, mastitis, tonsillitis, typhoid, meningitis, infections of the nervous system, salpingitis, endometritis, genital infections, pelveoperitonitis and eye infections (EP 350 733 Bl, US 4 990 517, 5 607 942 and WO 01/45679). -2- The principal indications for moxifloxacin are diseases of the respiratory tract, especially of the lungs. Dosage forms for moxifloxacin mentioned in EP-B 350 733 are tablets, coated tablets, capsules, pills, granules, suppositories, solutions, suspensions and emulsions, pastes, ointments, gels, 5 creams, lotions, dusting powders and sprays. To our knowledge, only tablets and (for intravenous administration) solutions are on the market. In practice, moxifloxacin has to date been used exclusively systemically for all diseases for the control of which it is suitable (including those of the lungs). The reason for this is the high oral bioavailability and the good distribution of the active ingredient. Although the increase in the 10 active ingredient concentration in the serum and lungs of rats after local (intratracheal) administration of moxifloxacin hydrochloride is greater than with systemic (oral) administration of the same amount of moxifloxacin hydrochloride, its concentration also falls relatively rapidly (within about an hour) to the level of the concentration reached orally, so that intratracheal local administration achieves no advantages compared with oral administration in experiments on rats Ciprofloxacin hydrochloride and enrofloxacin hydrochloride (II) are antibacterial quinolonecarboxylic acid derivatives which have been known for about 20 years (EP-B 49 355, US-A 4 670 444) and which can be employed extremely successfully both for the prophylaxis and for the treatment of systemic and local bacterial infections, especially of the urinary tract. 20 Ciprofloxacin is also effective inter alia against anthrax pathogens. The dosage forms of ciprofloxacin/enrofloxacin mentioned in EP-B 49 355 are tablets, coated tablets, capsules, pills, granules, suppositories, solutions, suspensions and emulsions, pastes, ointments, gels, creams, lotions, dusting powders and sprays. Ciprofloxacin tablets, suspensions, 25 eye and ear drops and solutions suitable for intravenous infusion are currently on the market. It has been found, surprisingly, that control of diseases of the respiratory organs, especially lung diseases caused by bacteria, is extremely successful when ciprofloxacin or enrofloxacin is administered locally as solid betaine and/or as solid slightly soluble betaine salt. The active 15 too. O (ID ciprofloxacin hydrochloride: R = H enrofloxacin hydrochloride: R = C2H5 -3 - ingredient concentration in the lungs can be kept for a lengthy period at a level desirable from the medical viewpoint for optimal treatment. Besides the higher and long-lasting active ingredient level at the site of the infection, it is possible to achieve simultaneously a comparatively low systemic concentration of the active ingredient, so that side effects of the medication and the 5 disquieting development of resistance through systemic selection pressure are at least drastically reduced or even entirely prevented in this way. The invention therefore relates to a method for controlling diseases of the respiratory organs, especially lung diseases caused by bacteria, in humans and animals by local administration of an antibacterially effective amount of solid betaine of the formula (III) and/or of its solid slightly soluble salt and to the use of these compounds for producing medicaments for the local control of diseases of the respiratory organs, especially lung diseases caused by bacteria, in humans and animals, where the compounds are administered in solid form. "Slightly soluble salts" for the purposes of the invention have a solubility in water of less than 0.1, 15 preferably less than 0.01, % by weight based on water at 25°C and a pH of 7. Such slightly soluble salts include Cit-Cig fatty acid salts of the betaine (III) and salts of the betaine (III) with acids such as, for example, the embonates or else salts of the betaine (III) with bases such as N,N'-dibenzylethylenediamine. The invention relates in a preferred embodiment to a method for controlling diseases of the 20 respiratory organs, especially lung diseases caused by bacteria, in humans and animals by local administration of an antibacterially effective amount of solid betaine of the formula (III) and/or its embonate and to the use of these compounds for producing medicaments for the local control of diseases of the respiratory organs, especially lung diseases caused by bacteria, in humans and animals, where the compounds are administered in solid form. O (III) 10 R = H, C2H5 25 In a particular embodiment of the invention, the diseases of the respiratory organs comprise diseases, caused by bacteria, of the airways or of the lungs, especially lung dieases caused by bacteria. -4- The embonates (also called pamoates) are salts of embonic acid, corresponding to formula (IV a) and/or (IV b): The term "embonate" refers for the purposes of the invention to the embonate, the hemiembonate and 5 to mixtures thereof. The term "respiratory organs" (or respiratory system) refers for the purposes of the invention to the nose, oral cavity and pharynx, and the larynx, trachea and lungs, including the airways and the paranasal sinuses and frontal sinus, where "airways" (or respiratory tract) mean the nasal cavity, oral cavity, pharynx, larynx, trachea and bronchi. 10 "Local administration" or "local control" in connection with diseases of the respiratory organs, especially lung diseases, means for the purposes of the invention - in contrast to oral administration of dosage forms intended for absorption via the gastrointestinal tract, and in contrast to intravenous administration - administration of the active ingredient by inhalation in inhalable dosage form. The preparation in powder form or powder-containing suspensions to be 15 used according to the invention are preparations which are aerosolized and then inhaled. (IVa) R = H, C2Hs COOH The term "inhalation" or "administration by inhalation" refers in this connection to the introduction into the respiratoiy organs, especially into and/or via the airways, preferably into and/or via the nasal cavity and oral cavity. -5- The term "intratracheal" or "intratracheal administration" refers for the purposes of the invention to introduction into the trachea not by inhalation, in particular for pulmonary disease control in experimental animals such as rats as a model of administration by inhalation. The invention further relates to devices which contain preparations containing betaine (III) and/or 5 its solid slightly soluble salt, in particular its embonate, and which are suitable for the administration by inhalation thereof in solid form, i.e. aerosolizers which are able to administer preparations containing betaine (III) and/or its solid slightly soluble salt, in particular its embonate, by inhalation in solid form (powder inhalers), or aersolizers which are able to administer suspensions containing betaine (III) and/or its solid slightly soluble salt, in particular its embonate, 10 in solid form by inhalation (suspension sprays). Solid preparations for dry powder inhalation or suspension inhalation will generally contain an amount of active ingredient (i.e. betaine (III) and/or its solid slightly soluble salt, in particular its embonate) which is as high as possible. The amount of active ingredient therein is usually at least 60, preferably at least 70, in particular at least 80 and most preferably at least 90, % by weight 15 based on the preparation ready for use. However, the amount of active ingredient therein may also be less than 60% by weight based on the preparation ready for use and is then preferably at least 30, in particular at least 40, % by weight based on the preparation ready for use. Where no adjuvants are necessary, especially in the case of solid preparations for suspension inhalation, they may also consist of active ingredient alone. However, for practical reasons, the preparations 20 according to the invention are often medicaments which, besides the active ingredient, contain one or more pharmacologically acceptable excipients. A review of various suitable preparations and corresponding administration aids is to be found for example in R. Stangl, "An Overview of Innovative Inhalation Devices", European Pharmaceutical Review, pages 50-55, (2002) and the literature cited therein. Pharmacologically acceptable excipients include, inter alia, binders (e.g. 25 maize starch, gelatin), stabilizers (e.g. antioxidants such as ascorbic acid), carriers (e.g. microcrystalline cellulose, lactose, sucrose, calcium phosphate, maize starch), lubricants (e.g. talc, stearic acid, magnesium stearate, calcium stearate or zinc stearate), flavourings and/or fragrances. The production of suitable preparations by selecting suitable excipients in terms of nature and quantity is straightforward. 30 The preparations according to the invention can be produced - as is usual in the production of inhalable free-flowing medicaments in powder form, by micronizing the active ingredient or by spray drying appropriate solutions or suspensions. The solid preparations generally have a particle diameter, determined as volume median (with the aid of a laser diffraction apparatus), of from 0.2 to 15 fim, preferably from 1 to 5 ^m. The diameter -6- determined as volume median is the value below and above which 50% of the volume of the particles lie. In a preferred embodiment, the solid preparations have particle diameters, determined as 50% of volume median, of from 2 to 5 pm and particle diameters, determined as 90% volume proportion, 5 of from 6 to 10 pm. In a further preferred embodiment, the solid preparations contain active ingredient, in particular ciprofloxacin betaine, with a particle diameter, determined as 50% volume median, of from 2 to 5 pm and particle diameters, determined as 90% volume proportion, of from 6 to 10 |im. The diameter determined as 50% or 90% volume proportion (with the aid of a laser diffraction apparatus) is the value below which respectively 50% and 90% of the volume of the 10 particles lie. Thus, for example, in a solid preparation with a particle diameter, determined as 50% volume median, of 2 pm and a particle diameter, determined as 90% volume proportion, of 6 pm (50% < 2 pm; 90% < 6 pm) the particle diameter of 50% of the volume of the particles is below 2 pm and of 90% of the volume of the particles is below 6 pm. It has generally proved advantageous in administration by inhalation to administer amounts of 15 about 0.1 to 20, preferably about 0.5 to 7.5, mg/kg of bodyweight to achieve effective results. It may nevertheless be necessary to depart from the stated amounts, specifically as a function of the bodyweight, individual behaviour towards the active ingredient, nature of the preparation and time or interval over which administration takes place. Thus, it may suffice in some cases to make do with less than the aforementioned minimum amount, whereas in other cases the said upper limit 20 must be exceeded. Where larger amounts are administered, it may be advisable to divide them into a plurality of single doses over the day. Examples Preparation of ciprofloxacin embonate a) Ciprofloxacin embonate (IV a; R = H) 33.1 g (0.1 mol) of ciprofloxacin betaine and 38.8 g (0.1 mol) of embonic acid are heated in 500 ml of glycol monomethyl ether under reflux for 1 hour. After cooling, the precipitate is filtered off with suction, thoroughly washed with ethanol and dried at 120°C under high vacuum. b) Ciprofloxacin hemiembonate (IV b: R = H) 66.2 g (0.2 mol) of ciprofloxacin betaine and 38.8 g (0.1 mol) of embonic acid are heated in 500 ml of glycol monomethyl ether under reflux for 1 hour. After cooling, the precipitate is filtered off with suction, thoroughly washed with ethanol and dried at 120°C under high vacuum. Determination of the active ingredient concentration in the lungs of rats Female Wistar rats (80 to 100 g) were treated with A1 - 7.5 mg/kg ciprofloxacin betaine (laboratory product) intratracheally as suspension; A2 - 7.5 mg/kg ciprofloxacin betaine (micronized: 50% < 3 |im; 90% < 7 jxm) intratracheally as suspension; B - 7.5 mg/kg ciprofloxacin hydrochloride intratracheally as solution; C - 7.5 mg/kg ciprofloxacin-hydrochloride intravenously as solution. Three animals from each of the dose groups were sacrificed after 0.25, 0.5, 1, 3 and 5 hours, and the lungs were removed. The lungs were homogenized using a Plotter from Braun. The active ingredient content in the lung homogenates was determined by bioassay. Pharmacokinetic parameters for the lungs Dose group AUC [mg*h/l] Cm„ [mg/1] Unlh] A1 124 49.1 1.96 A2 304 76 13.47 B 3.20 6.65 0.847 C 0.497 0.610 0.758 -8- Lung concentrations in fig/ml; averages for 3 animals Dose group 0.25 h 0.5 h 1 h 3 h 5 h A1 49.1 44.3 40.1 12.6 7.21 A2 76 76 76 54 54 B 6.65 1.67 0.63 0.10 0 C 0.61 0.35 0.14 0 0 AUC, Craax and ti/2 are important pharmacokinetic parameters for describing pharmacokinetic/pharmacodynamic interactions; cf., for example, W.A. Craig, 5 "Pharmacokinetic/pharmacodynamic parameters: rationale for antibacterial dosing of mice and men", Clin. Infect. Dis. 26, 1-12 (1998). Intratracheal administration of ciprofloxacin-betaine (laboratory product) reveals, compared with intratracheal administration of ciprofloxacin-hydrochloride, a 40 times larger AUC and an 8 times higher Cmax. This kinetic advantage becomes even clearer on comparison with intravenous 10 administration of ciprofloxacin hydrochloride (AUC: factor 250, Craax: factor 80). Intratracheal administration of micronized ciprofloxacin-betaine with a particle diameter (50 % < 3 urn; 90 % < 7 urn) leads to a further improvement in the pharmacokinetic profile (AUC: factor 612, Cmax: factor 125, compared with intravenous administration of ciprofloxacin hydrochloride). Efficacy in a model of lung infection with P. aeruginosa 15 Female Wistar rats (80 to 100 g) were infected intratracheally with P. aeruginosa DSM 12055 and treated 1 and 4 hours after the infection with ciprofloxacin betaine (laboratory product) intratracheally (i.t.) and with ciprofloxacin hydrochloride intratracheally and intravenously (i.v.). Various dose groups each of 5 rats were employed. The animals were sacrificed 24 hours after the infection, and the lungs were removed and homogenized with a Potter from Braun. The 20 homogenates were plated out to determine the microbe count in the lungs. The following table shows the reduction in the microbe count in the lungs (log units) after 24 h relative to the untreated infection control (in each case averages for 5 animals): </div>

Claims

<div class="application article clearfix printTableText" id="claims">



-9- 

Dose group 

Reduction in microbe count (log units) 

A - 0.8 mg/kg ciprofloxacin betaine i.t. 

-4.0 

B - 2.5 mg/kg ciprofloxacin betaine i.t. 

-5.8 

C - 7.5 mg/kg ciprofloxacin betaine i.t. 

-10 

D - 0.8 mg/kg ciprofloxacin hydrochloride i.t. 

-1.8 

E - 2.5 mg/kg ciprofloxacin hydrochloride i.t. 

-1.1 

F - 7.5 mg/kg ciprofloxacin hydrochloride i.t. 

-2.8 

G - 2.5 mg/kg ciprofloxacin hydrochloride i.v. 

-2.8 

H - 7.5 mg/kg ciprofloxacin hydrochloride i.v. 

-3.5 

I - 22.5 mg/kg ciprofloxacin hydrochloride i.v. 

-5.4 

J - 67.5 mg/kg ciprofloxacin hydrochloride i.v. 

-8.8 

Intratracheal use of ciprofloxacin betaine leads to a reduction of from 4 to 10 log units in the microbe count in the lungs in all three dose groups, whereas equal dosages of ciprofloxacin 5 hydrochloride administered intratracheally bring about a far smaller reduction in the microbe count (1.1 to 2.8 log units). Although intravenous administration of ciprofloxacin hydrochloride, the current state of the art, also leads to a marked reduction in the microbe count in the lungs (2.8 to 8.8 log units), this is only with dosages which are 10 times higher. The treatment according to the invention thus leads to a greatly reduced systemic exposure. 

10 In a further test with P.aeruginosa DSM 12055, a single intratracheal treatment (1 hour after the infection) was carried out with micronized ciprofloxacin betaine as dry powder. A dose of 10 mg/kg was administered with the aid of a DP-3 dry powder insufflator (PENN-CENTURY, INC.). It is known from control investigations that about 5 to 20% of the administered dose reach the lungs. In this experiment, the microbe count in the lungs was reduced by more than 6 log units 15 compared with an untreated control group. 

- 10-
2.
3.
4.
5.
6. 

we claim is: 

A method for controlling bacterial diseases of the respiratory organs in non-human animals by local administration of an antibacterially effective amount of solid ciprofloxacin of the formula (III) 

wherein R = H. 

The method according to Claim 1 for controlling lung diseases caused by bacteria. 

The use of solid ciprofloxacin of the formula (III) 

wherein R = H; 

for producing a medicament for the local control of bacterial diseases of the respiratory organs; wherein the medicament is formulated for the administration of the ciprofloxacin compound in solid form. 

The use according to Claim 3 for the local control of lung diseases caused by bacteria. 

The use according to Claim 3 or 4 for the local control of cystic fibrosis. 

The use according to Claim 3 or 4 for the local control of chronic obstructive pulmonary diseases (COPD). 

O 

(III) 

-11 -
7.
8.
9.
10.
11. 

A device suitable for administration by inhalation of solid active ingredient; wherein the device includes a preparation that comprises the ciprofloxacin compound defined in Claim 1. 

A device according to Claim 7, designed as a powder inhaler. 

A method according to Claim 1, substantially as herein described or exemplified. 

A use according to Claim 3, substantially as herein described or exemplified. 

A device according to Claim 7, substantially as herein described or exemplified. 



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